Huang LQ - Search Results

1

[Translational frameshift may be occur in p11, an interaction protein of Cx31, in yeast].

Huang LQ, Shi XL, Tan ZP, Fang HY, Zheng D, Xia JH, Xia K. Huang LQ, et al. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2002 Mar;34(2):219-24. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2002. PMID: 12007000 Chinese.

2

[Expression and purification of p11 fusion protein in E. coli and preparation of antiserum against GST-p11].

Tan ZP, Huang LQ, Zheng D. Tan ZP, et al. Among authors: huang lq. Hunan Yi Ke Da Xue Xue Bao. 2002 Jun 28;27(3):189-91. Hunan Yi Ke Da Xue Xue Bao. 2002. PMID: 12575286 Chinese.

3

Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells.

He LQ, Liu Y, Cai F, Tan ZP, Pan Q, Liang DS, Long ZG, Wu LQ, Huang LQ, Dai HP, Xia K, Xia JH, Zhang ZH. He LQ, et al. Among authors: huang lq. Acta Biochim Biophys Sin (Shanghai). 2005 Aug;37(8):547-54. doi: 10.1111/j.1745-7270.2005.00080.x. Acta Biochim Biophys Sin (Shanghai). 2005. PMID: 16077902 Free article.

4

[Interaction of connexin 26 with the C-terminal of neuroendocrine specific protein].

Xiao ZA, Xie DH, Huang LQ, Shi XL, Xia K, Yang S, Xia JH. Xiao ZA, et al. Among authors: huang lq. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2004 Aug;29(4):401-4, 418. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 16134590 Chinese.

5

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ. Xia JH, et al. Nat Genet. 1998 Dec;20(4):370-3. doi: 10.1038/3845. Nat Genet. 1998. PMID: 9843210

6

[Localization of the gene for 4 hereditary multiple exostoses families].

Tang Y, Xia JH, Zhou JN, Li HJ, Wang DP, Dai HP, Long ZG, Tang BS, Huang L, Deng HX. Tang Y, et al. Yi Chuan Xue Bao. 1998;25(1):1-7. Yi Chuan Xue Bao. 1998. PMID: 9648398 Chinese.

7

[Molecular cloning of EXT2 and EXT4 gene].

Deng H, Xu L, Ruan Q, Huang L, Xia J. Deng H, et al. Hunan Yi Ke Da Xue Xue Bao. 1998;23(6):519-23. Hunan Yi Ke Da Xue Xue Bao. 1998. PMID: 10806756 Chinese.

8

Sequencing for 4 single-copy DNA segments from human chromosome 8q24.1.

Xia JH, Ruan QG, He XX, Li LL, Huang L, Deng HX, Li LY. Xia JH, et al. Chin Med J (Engl). 1994 Apr;107(4):257-9. Chin Med J (Engl). 1994. PMID: 8088191

9

Trafficking abnormality and ER stress underlie functional deficiency of hearing impairment-associated connexin-31 mutants.

Xia K, Ma H, Xiong H, Pan Q, Huang L, Wang D, Zhang Z. Xia K, et al. Protein Cell. 2010 Oct;1(10):935-43. doi: 10.1007/s13238-010-0118-7. Epub 2010 Nov 9. Protein Cell. 2010. PMID: 21204020 Free PMC article.

10

Isolation and characterization of a new chromosome 8q24.1 band-specific microsatellite polymorphism.

Xu L, Xia J, Tang Y, Pan Q, Huang L, Deng H. Xu L, et al. Hunan Yi Ke Da Xue Xue Bao. 1997;22(6):471-4. Hunan Yi Ke Da Xue Xue Bao. 1997. PMID: 10072981

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